logo
AAT Bioquest

Buccutite™ Rapid PE-iFluor® 710 Tandem Antibody Labeling Kit *Microscale Optimized for Labeling 100 ug Antibody Per Reaction*

Product key features

  • Streamlined Two-Step Protocol - Directly labels antibodies or proteins in under two hours with a two-step process
  • Optimized for Small-Scale Labeling - Optimized for 100 µg of purified antibody or protein per reaction
  • High Fluorescence Sensitivity - PE-iFluor® 710 offers strong fluorescence and a large Stokes shift, ideal for multicolor flow cytometry
  • Enhanced Experimental Flexibility - Eliminates the need for secondary antibodies, providing greater flexibility for multicolor panel design

Product description

  • The Buccutite™ Rapid PE-iFluor® 710 Tandem Antibody Labeling Kit offers a highly efficient and reproducible method for small-scale conjugation of antibodies with PE-iFluor® 710. Utilizing the advanced Buccutite™ crosslinking platform, this kit significantly simplifies the labeling workflow compared to conventional strategies such as SMCC-mediated crosslinking. The streamlined two-step protocol allows for the rapid conjugation of antibodies or proteins to PE-iFluor® 710 in under two hours, with minimal hands-on time.

    Each kit includes all reagents necessary for two labeling reactions, with each reaction optimized to conjugate 100 µg of purified antibody or protein using Buccutite™ FOL-Activated PE-iFluor® 710. For optimal performance, the removal of stabilizing proteins (e.g., BSA) and avoidance of amine-containing buffers such as Tris are critical, as these components can interfere with the conjugation chemistry.

    PE-iFluor® 710 is a tandem fluorophore with excitation and emission maxima at ~565 nm and ~747 nm, respectively, offering a substantial Stokes shift and high fluorescence intensity. These properties make it particularly well-suited for applications such as multicolor flow cytometry, spectral flow cytometry, and other fluorescence-based immunoassays requiring high sensitivity. However, due to its limited photostability, it is not recommended for applications involving prolonged light exposure. This kit enables direct labeling of primary antibodies, eliminating the need for secondary antibody-based detection systems. The resulting conjugates reduce experimental complexity and enhance assay sensitivity and reproducibility.

Example protocol

AT A GLANCE

Protocol Summary
  1. Add 5 µL Reaction Buffer (Component C) into antibody (100 µL)

  2. Add the antibody solution into Buccutite™ MTA vial (Component B)

  3. Incubate at room temperature for 30 minutes

  4. Mix with 50 µL Buccutite™ FOL-Activated PE-iFluor® 710 (Component A)

  5. Incubate at room temperature for 60 minutes

Important: Store the kit at 4 °C upon receipt. When stored correctly, the kit remains stable for six months. Alternatively, Component B can be stored at -20 °C. Avoid freezing Buccutite™ FOL-Activated PE-iFluor® 710 (Component A) and Reaction Buffer (Component C). Before use, warm all components to room temperature and briefly centrifuge the vials before opening. Prepare the necessary solutions immediately prior to starting the conjugation. The following SOP provides an example for labeling goat anti-mouse IgG antibody.

PREPARATION OF WORKING SOLUTION

Antibody Working Solution
  1. To label 100 µg of antibody (assuming a concentration of 1 mg/mL), mix 5 µL (5% of the total reaction volume) of Reaction Buffer (Component C) with 100 µL of the antibody solution.

    Note: If your antibody has a different concentration, adjust the volume to ensure approximately 100 µg of antibody is available for the labeling reaction.

    Note: The antibody should be dissolved in 1X phosphate buffered saline (PBS), pH 7.2-7.4; If the antibody is dissolved in glycine buffer, it must be dialyzed against 1X PBS, pH 7.2-7.4, or use ReadiUse™ 10KD Spin Filter (Cat. # 60502 from AAT Bioquest) to remove free amines or ammonium salts (such as ammonium sulfate and ammonium acetate) that are widely used for antibody precipitation.

    Note: Impure antibodies or antibodies stabilized with bovine serum albumin (BSA) or gelatin will not be labeled well.

    Note: The antibody –Buccutite™ MTA reaction efficiency is significantly reduced if the antibody concentration is less than 1 mg/mL. For optimal labeling efficiency the final antibody concentration range of 1-10 mg/mL is recommended.

SAMPLE EXPERIMENTAL PROTOCOL

Run Antibody-Buccutite™ MTA Reaction
  1. Add the antibody working solution directly into the vial of Buccutite ™ MTA (Component B), and mix them well by repeatedly pipetting for a few times or vortex the vial for a few seconds.
  2. Keep the antibody- Buccutite ™ MTA reaction mixture at room temperature for 30 - 60 minutes.

    Note: The antibody-Buccutite™ MTA reaction mixture can be rotated or shaken for longer time if desired.

Make Antibody-PE-iFluor® 710 Conjugation
  1. Make Buccutite™ FOL-Activated PE-iFluor® 710 solution by adding 50 µL ddH2O into the vial of Buccutite™ FOL-Activated PE-iFluor® 710 (Component A), mix well by repeatedly pipetting for a few times or vortex the vial for a few seconds.

  2. Mix whole vial of Buccutite™ FOL-Activated PE-iFluor® 710 solution into the antibody-Buccutite™ MTA solution, mix well and rotating the mixture for 1 hour at room temperature.

  3. The antibody-PE-iFluor® 710 conjugate is now ready to use.

    Note: For immediate use, the antibody-PE-iFluor® 710 conjugate need be diluted with the buffer of your choice.

Storage of Antibody-PE-iFluor® 710 Conjugate

The antibody conjugate should be stored at > 0.5 mg/mL in the presence of a carrier protein (e.g., 0.1% bovine serum albumin). The Antibody-PE-iFluor® 710 conjugate solution could be stored at 4 °C for two months without significant change when stored in the presence of 2 mM sodium azide and kept from light. For longer storage, the antibody-PE-iFluor® 710 conjugates could be lyophilized and stored at ≤ –20 °C.

Table 1. Available fluorophores at AAT Bioquest Buccutite™ Rapid Antibody Labelling Kits

Cat#LabelsEx (nm)Em (nm)
1325PerCP482677
1310PE565575
1318PE-Texas Red565600
1356PE-iFluor® 594565606
1322PE-Cy5565674
1316PE-Cy5.5565700
1358PE-iFluor® 710565710
1317PE-Cy7565780
1311APC651662
1320APC-Cy5.5651700
1319APC-iFluor® 700651713
1321APC-Cy7651780

 

Spectrum

References

View all 8 references: Citation Explorer
Multiplexed non-invasive tumor imaging of glucose metabolism and receptor-ligand engagement using dark quencher FRET acceptor.
Authors: Rudkouskaya, Alena and Sinsuebphon, Nattawut and Ochoa, Marien and Chen, Sez-Jade and Mazurkiewicz, Joseph E and Intes, Xavier and Barroso, Margarida
Journal: Theranostics (2020): 10309-10325
Performance of optoacoustic and fluorescence imaging in detecting deep-seated fluorescent agents.
Authors: Chen, Zhenyue and Deán-Ben, Xosé Luís and Gottschalk, Sven and Razansky, Daniel
Journal: Biomedical optics express (2018): 2229-2239
An enzymatically-sensitized sequential and concentric energy transfer relay self-assembled around semiconductor quantum dots.
Authors: Samanta, Anirban and Walper, Scott A and Susumu, Kimihiro and Dwyer, Chris L and Medintz, Igor L
Journal: Nanoscale (2015): 7603-14
Multicolor detection of rare tumor cells in blood using a novel flow cytometry-based system.
Authors: Watanabe, Masaru and Uehara, Yuri and Yamashita, Namiko and Fujimura, Yuu and Nishio, Kaori and Sawada, Takeshi and Takeda, Kazuo and Koizumi, Fumiaki and Koh, Yasuhiro
Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology (2014): 206-13
Noninvasive and quantitative assessment of in vivo fetomaternal interface angiogenesis using RGD-based fluorescence.
Authors: Keramidas, M and Lavaud, J and Sergent, F and Hoffmann, P and Brouillet, S and Feige, J-J and Coll, J-L and Alfaidy, N
Journal: BioMed research international (2014): 309082
Page updated on December 17, 2024

Ordering information

Price
Unit size
Catalog Number1358
Quantity
Add to cart

Additional ordering information

Telephone1-800-990-8053
Fax1-800-609-2943
Emailsales@aatbio.com
InternationalSee distributors
Bulk requestInquire
Custom sizeInquire
Technical SupportContact us
Purchase orderSend to sales@aatbio.com
ShippingStandard overnight for United States, inquire for international
Request quotation

Spectral properties

Absorbance (nm)

566

Extinction coefficient (cm -1 M -1)

1960000

Excitation (nm)

565

Emission (nm)

747

Storage, safety and handling

H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22
UNSPSC12171501

Components

AAT Bioquest offers the Buccutite™ rapid labeling kit to streamline PE tandem dye conjugation for antibodies and other proteins, including streptavidin and secondary reagents. This kit utilizes preactivated PE modified with Buccutite™ FOL, while your antibody or protein is modified with Buccutite™ MTA to produce MTA-modified proteins. The MTA-modified proteins react efficiently with FOL-modified PE, yielding the desired PE-antibody conjugate with significantly higher efficiency compared to traditional SMCC chemistry. Additionally, the reaction requires much lower biopolymer concentrations, enhancing efficiency and reducing material usage compared to SMCC-based methods.
AAT Bioquest offers the Buccutite™ rapid labeling kit to streamline PE tandem dye conjugation for antibodies and other proteins, including streptavidin and secondary reagents. This kit utilizes preactivated PE modified with Buccutite™ FOL, while your antibody or protein is modified with Buccutite™ MTA to produce MTA-modified proteins. The MTA-modified proteins react efficiently with FOL-modified PE, yielding the desired PE-antibody conjugate with significantly higher efficiency compared to traditional SMCC chemistry. Additionally, the reaction requires much lower biopolymer concentrations, enhancing efficiency and reducing material usage compared to SMCC-based methods.
AAT Bioquest offers the Buccutite™ rapid labeling kit to streamline PE tandem dye conjugation for antibodies and other proteins, including streptavidin and secondary reagents. This kit utilizes preactivated PE modified with Buccutite™ FOL, while your antibody or protein is modified with Buccutite™ MTA to produce MTA-modified proteins. The MTA-modified proteins react efficiently with FOL-modified PE, yielding the desired PE-antibody conjugate with significantly higher efficiency compared to traditional SMCC chemistry. Additionally, the reaction requires much lower biopolymer concentrations, enhancing efficiency and reducing material usage compared to SMCC-based methods.